Continuous, Real-Time Monitoring of Cocaine in Undiluted Blood Serum via a Microfluidic, Electrochemical Aptamer-Based Sensor

被引:310
作者
Swensen, James S. [1 ,2 ]
Xiao, Yi [1 ,2 ]
Ferguson, Brian S. [2 ]
Lubin, Arica A. [3 ]
Lai, Rebecca Y. [3 ,4 ]
Heeger, Alan J. [1 ,4 ]
Plaxco, Kevin W. [3 ,5 ]
Soh, H. Tom. [1 ,2 ,5 ]
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mech Engn, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[5] Univ Calif Santa Barbara, Grad Program BioMol Sci & Engn, Santa Barbara, CA 93106 USA
基金
美国国家卫生研究院;
关键词
IN-VITRO SELECTION; ELECTRONIC DETECTION; SMALL-MOLECULE; DNA; OLIGONUCLEOTIDES; REAGENTLESS; PROBE;
D O I
10.1021/ja806531z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of a biosensor system capable of continuous, real-time measurement of small-molecule analytes directly in complex, unprocessed aqueous samples has been a significant challenge, and successful implementation has been achieved for only a limited number of targets. Toward a general solution to this problem, we report here the Microfluidic Electrochemical Aptamer-based Sensor (MECAS) chip wherein we integrate target-specific DNA aptamers that fold, and thus generate an electrochemical signal, in response to the analyte with a microfluidic detection system. As a model, we demonstrate the continuous, real-time (similar to 1 min time resolution) detection of the small-molecule drug cocaine at near physiological, low micromolar concentrations directly in undiluted, otherwise unmodified blood serum. We believe our approach of integrating folding-based electrochemical sensors with miniaturized detection systems may lay the groundwork for the real-time, point-of-care detection of a wide variety of molecular targets.
引用
收藏
页码:4262 / 4266
页数:5
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